What is Limb conditions?

What is Limb conditions?

• Limb conditions: Medical conditions affecting the upper or lower limbs.

Limb conditions: Introduction

Types of Limb conditions:

Types of Limb conditions:

• Extradural hematoma
• Broken finger
• Broken foot
• Foot fracture
• Broken hand
• Hand fracture
• Broken leg
• Fractured femur
• Broken toe
• Dislocated elbow
• Spastic Paraplegia 42, Autosomal Dominant
• Acral lentiginous melanoma
• Spastic paraplegia 30, autosomal recessive
• Spastic paraplegia 32, autosomal recessive
• Spastic paraplegia 33, autosomal dominant
• Neuropathy sensory spastic paraplegia
• Spastic paraplegia 3, autosomal dominant
• Charcot-Marie-Tooth disease, X-linked recessive, 2
• Spastic paraplegia 4, autosomal dominant
• Charcot-Marie-Tooth disease, X-linked recessive, 3
• Spastic paraplegia 8, autosomal dominant
• Spastic paraplegia 9, autosomal dominant
• Charcot-Marie-Tooth disease, Type 2AII
• Charcot-Marie-Tooth disease, Type 1A
• Charcot-Marie-Tooth disease, Type 1B
• Charcot-Marie-Tooth disease, Type 2B
• Charcot-Marie-Tooth disease, Type 1C
• Charcot-Marie-Tooth disease, Type 4A
• Charcot-Marie-Tooth disease, Type 2C
• Charcot-Marie-Tooth disease, Type 1D
• Charcot-Marie-Tooth disease, Type 2D
• Charcot-Marie-Tooth disease, Type 1E
• Charcot-Marie-Tooth disease, Type 4C
• Charcot-Marie-Tooth disease, Type 2E
• Charcot-Marie-Tooth disease, Type 1F
• Charcot-Marie-Tooth disease, Type 2G
• Charcot-Marie-Tooth disease, Type 4E
• Charcot-Marie-Tooth disease, Type 4F
• Charcot-Marie-Tooth disease, Type 2H
• Charcot-Marie-Tooth disease, Type 4G
• Spastic paraplegia type 5A, recessive
• Charcot-Marie-Tooth disease, Type 2I
• Charcot-Marie-Tooth disease, Type 4H
• Spastic paraplegia type 5B, recessive
• Charcot-Marie-Tooth disease, Type 2J
• Charcot-Marie-Tooth disease, type 2
• Charcot-Marie-Tooth disease, Type 2A
• Charcot-Marie-Tooth disease, type 4
• Charcot-Marie-Tooth disease, demyelinating, autosomal dominant
• Charcot-Marie-Tooth, demyelinating, autosomal recessive
• Charcot-Marie-Tooth disease, X-linked
• Charcot-Marie-Tooth disease, type 1
• Charcot-Marie-Tooth disease, Type 2L
• Spastic paraplegia 24
• Foot conditions
• Leg conditions
• Knee conditions
• Elbow conditions
• Finger conditions
• Wrist conditions
• Shoulder conditions
• Psoriasis on Eblows and Knees
• Psoriasis on trunk and limbs
• Palmoplantar Psoriasis
• Spinal Muscular Atrophy
• Spinal Muscular Atrophy type I
• Spinal Muscular Atrophy type II
• Spinal Muscular Atrophy type III
• Adult SMA
• Muscular Dystrophy
• Duchenne Muscular Dystrophy
• Becker Muscular Dystrophy
• Limb-girdle Muscular Dystrophy
• Muscular dystrophy, Duchenne and Becker type
• Adult progressive spinal muscular atrophy, Aran Duchenne type
• Becker's muscular dystrophy (BMD)
• Muscular dystrophy, limb-girdle, autosomal recessive, type 2K
• Muscular dystrophy, limb-girdle, autosomal dominant, type 1F
• Muscular dystrophy, limb-girdle, autosomal dominant, type 1G
• Muscular dystrophy, limb-girdle -- mental retardation
• Limb-girdle muscular dystrophy type 1B
• Limb-Girdle muscular dystrophy type 2A
• Limb-girdle muscular dystrophy type 1A
• Limb-girdle muscular dystrophy type 2B
• Limb-girdle muscular dystrophy type 1C
• Limb-girdle muscular dystrophy type 2C
• Limb-girdle muscular dystrophy type 1D
• Limb-girdle muscular dystrophy type 2D
• Limb-girdle muscular dystrophy type 1E
• Limb-girdle muscular dystrophy type 2E
• Limb-girdle muscular dystrophy type 2F
• Limb-girdle muscular dystrophy type 2G
• Limb-girdle muscular dystrophy type 2H
• Limb-girdle muscular dystrophy type 2I
• Muscular dystrophy, limb girdle
• Myasthenia, familial limb-girdle
• Muscular dystrophy, limb-girdle, autosomal dominant
• Myopathy, limb-girdle, with bone fragility
• Muscular dystrophy, limb-girdle type 2M
• Muscular dystrophy limb girdle type 2A, Erb type
• Muscular dystrophy, limb-girdle, autosomal recessive, type 2H
• Muscular dystrophy, limb-girdle, autosomal recessive, type 2B
• Muscular dystrophy, limb girdle, autosomal recessive, type 2A
• Muscular dystrophy, limb-girdle, autosomal recessive, type 2E
• Myasthenia, Limb-Girdle, with Tubular Aggregates
• Shoulder and girdle defect -- mental retardation, familial
• Muscular Dystrophy, Limb-Girdle, Type 3
• Limb-girdle Muscular Dystropy type 1B
• Autosomal recessive limb-girdle muscular dystrophy, type 2G
• Muscular dystrophy limb-girdle (generic term)
• Restless Legs Syndrome, Susceptibility To, 7
• Restless Legs Syndrome, Susceptibility To, 6
• Restless Legs Syndrome, Susceptibility To, 5
• Restless Legs Syndrome, Susceptibility To, 4
• Restless Legs Syndrome, Susceptibility To, 3
• Restless Legs Syndrome, Susceptibility To, 2
• Restless Legs Syndrome, Susceptibility To, 1
• Charcot-Marie-Tooth disease, X-linked, 1
• Onychodystrophy -- deafness
• Spinal muscular atrophy, Adult form
• Shoulder tendinitis
• Achilles tendinitis
• Knee tendinitis
• Shoulder impingement syndrome
• Shoulder bursitis
• Shoulder arthritis
• Impingement syndrome
• Seronegative spondyloarthropathy
• Knee osteoarthritis
• Finger osteoarthritis
• Wrist osteoarthritis
• Paralysis
• Paraplegia
• Legg-Calve-Perthes disease
• Flat feet
• Foot sprain
• Leg injury
• Thigh conditions
• Knee injury
• Knee arthritis
• Chondromalacia
• Osgood-Schlatter Disease
• Wrist injury
• Seal finger syndrome
• Triphalangeal thumb
• Ivory Epiphyses
• Supernumeracy Carpal Bones
• Carpal Fusion
• Carpal Synostosis
• Tarsal Fusion
• Tarsal Synostosis
• Inherited Acroosteolysis, phalangeal type
• Acquired Acroosteolysis, phalangeal type
• Acroosteolysis
• Acroosteolysis, phalangeal type
• Brachymetatarsalia
• Brachymetatarsalism
• Brachymetacarpalism
• Brachymetacarpalia
• Ulnar Ray Deficiency
• Radial Ray Deficiency
• Terminal Transverse Defect
• Angel-Shaped Phalanges
• Macrodactyly
• Fromont Anomaly
• Polydactyly, Preaxial 1
• Polydactyly, Preaxial 2
• Polydactyly, Preaxial 3
• Hyperpigmentation of fingers
• Hyperpigmentation of nails
• Autosomal recessive spastic paraplegia, type 11
• Decreased range of motion
• Decreased mobility
• Charcot-Marie-Tooth disease (generic term)
• Nail psoriasis
• Primary restless leg syndrome
• Secondary restless leg syndrome
• Carpal tunnel syndrome pain
• Phantom limb pain
• Mental retardation -- short stature -- hand contractures -- genital anomalies
• Armpit Boil
• Thigh Boil
• Raynaud's phenomenon
• Hammer toe
• Bunions
• Bunionette
• Ingrown nails
• Ingrown toenail
• Ankle conditions
• Sprain
• Osteoarthritis
• Gout
• Infectious arthritis
• Reactive arthritis
• Tendinitis
• Arthrogryposis
• Thigh muscle strain
• Forearm muscle strain
• Joint injury -- knee
• Ankle Osteoarthritis
• Ankle injuries
• Ankle sprain
• Knee sprain
• Wrist sprain
• Acute gout
• Palmoplantar pustular psoriasis
• Pretibial Myxedema
• Achilles tendonitis
• Ulnar Neuropathy
• Hand eczema
• Shin splints
• Tarsal tunnel syndrome
• Hand neuropathy
• Restless Legs Syndrome
• Periodic limb movements in sleep
• Trigger finger
• Writer's cramp
• Tennis elbow
• Golfer's elbow
• Ulnar nerve injury
• Epicondylitis
• Charcot-Marie-Tooth disease, X-linked recessive, 4
• Marfan Syndrome type 2
• Spastic paraplegia 6, autosomal dominant
• Charcot-Marie-Tooth disease, X-linked recessive, 5
• Microlissencephaly -- micromelia
• Shoulder Pain
• Tibial Fractures
• Bicep muscle strain
• Elbow sprain
• Toe sprain
• Radial Nerve Entrapment
• Finger Arthritis
• Skier's thumb
• Anterior Interosseous Nerve Compression
• Posterior Interosseous Nerve Syndrome
• Joint injury -- finger
• Elbow Osteoarthritis
• Toe Osteoarthritis
• Gamekeeper's thumb
• Finger sprain
• Calf muscle strain
• Hand muscle strain
• Ankle Arthritis
• Anterior Interosseous Nerve Syndrome
• Elbow Arthritis
• Shoulder sprain
• Toe Arthritis
• Radial Tunnel Syndrome
• Tricep muscle strain
• Joint injury -- ankle
• Shoulder muscle strain
• Joint injury -- elbow
• Upper arm muscle strain
• Wrist Arthritis
• Joint injury -- wrist
• Carpal spasm
• Psoriasis-like knee rash
• Diabetes like foot weakness
• Contact dermatitis -like behind-knee rash
• Ankle clonus
• Difficulty making fine hand movements
• Conditions associated with nail abnormalities
• Axillary lymphadenopathy
• Restless leg syndrome
• Pfeiffer Syndrome Type I
• Pfeiffer Syndrome Type II
• Pfeiffer Syndrome Type III
• Acrocephalosyndactyly Syndrome type 5
• Acrocephalosyndactyly type 5 (ACPS 5)
• Pfeiffer syndrome
• Pfeiffer syndrome Type 1
• Pfeiffer syndrome Type 2
• Pfeiffer syndrome Type 3
• Absence of tibia
• Absence of tibia with polydactyly
• Charcot-Marie-Tooth disease -- deafness
• Charcot-Marie-Tooth Disorder
• Charcot disease
• Charcot-Marie-Tooth disease, Type 2K
• Charcot-Marie-Tooth disease with ptosis and parkinsonism
• Charcot-Marie-Tooth type 1 aplasia cutis congenital
• Charcot-Marie-Tooth disease, Type 2B1
• Charcot-Marie-Tooth disease, Type 2B2
• Charcot-Marie-Tooth disease, Type 4B1
• Charcot-Marie-Tooth disease, Type 4B2
• Charcot-Marie-Tooth disease, Type 2AI
• Charcot-Marie-Tooth disease, dominant intermediate 1
• Charcot-Marie-Tooth disease, dominant intermediate 2
• Charcot-Marie-Tooth disease, dominant intermediate 3
• Spastic paraplegia type 1, X-linked
• Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma
• Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
• Charcot-Marie-Tooth disease deafness recessive type
• Charcot-Marie-Tooth disease, Type 2F
• Autosomal Dominant Charcot-Marie-Tooth with hearing loss
• Spastic Paraplegia 18, Autosomal Recessive
• Spastic paraplegia 11, autosomal recessive
• Spastic paraplegia 23
• Spastic paraplegia 17
• Spastic paraplegia 20, autosomal recessive
• Spastic paraplegia 14, autosomal recessive
• Spastic paraplegia 15, autosomal recessive
• Spastic paraplegia 25, autosomal recessive
• Spastic paraplegia 26, autosomal recessive
• Spastic paraplegia 16, X-linked
• Spastic paraplegia 10, autosomal dominant
• Spastic paraplegia 12, autosomal dominant
• Spastic paraplegia 13, autosomal dominant
• Spastic paraplegia 19, autosomal dominant
• Spastic paraplegia 29, autosomal dominant
• Spastic paraplegia 7, autosomal recessive
• Spastic paraplegia 39, autosomal recessive
• Spastic paraplegia 31, autosomal dominant
• Osgood Schlatter Condition
• Polydactyly preaxial
• Syndactyly type 1
• Syndactyly type 1 -- subtype 1
• Syndactyly type 1 -- subtype 2
• Syndactyly type 1 -- subtype 3
• Syndactyly type 1 -- subtype 4
• Syndactyly
• Osteogenesis imperfecta -- congenital joint contractures
• Amputation
• Foot injury
• Iliotibial Band Syndrome
• Plica Syndrome
• Knock knees
• Sclerodactyly
• Hand, Foot, & Mouth Disease
• Erythema nodosum
• Erythromelalgia
• Nail conditions
• Nail avulsion
• Ruptured achilles tendon
• Deep vein thrombosis
• Pill rolling hand movements
• Polydactyly
• Elbow injury
• Forearm injury
• Congenital short femur
• Split hand/split foot malformation, autosomal recessive
• Mental retardation, X-linked -- epilepsy -- progressive joint contractures -- typical face
• Nail dysplasia, isolated congenital
• Myopathy, Distal 3
• Myopathy, Distal 2
• Distal Myopathy 1
• Thumb sucking
• Foot ulcer
• Cramp
• Preaxial deficiency, postaxial polydactyly and hypospadias
• Preaxial deficiency postaxial polydactyly hypospadias
• Adducted thumbs -- arthrogryposis, Christian type
• Craniosynostosis -- brachysyndactyly of hands and absence of toes
• Ulnar hypoplasia with mental retardation
• Alopecia-contractures-dwarfism-mental retardation
• Blepharophimosis -- ptosis -- syndactyly -- mental retardation
• Brachydactyly -- mesomelia -- mental retardation -- heart defects
• Klippel Trenaunay Weber syndrome
• Klippel-Trenaunay Syndrome
• Brachydactyly -- anonychia
• Dwarfism, short-limb -- absent fibulas -- very short digits
• Mental mixed retardation -- deafness -- clubbed digits
• Severe mental retardation and absent nails of hallux and pollex
• Hypoplastic thumbs -- hydranencephaly
• Midphalangeal hair
• Pterygia -- mental retardation -- facial dysmorphism
• Deafness -- enamel hypoplasia -- nail defects
• Deafness -- hypospadias -- metacarpal and metatarsal synostosis
• Tibial aplasia -- ectrodactyly -- hydrocephalus
• Dandy-Walker malformation postaxial polydactyly
• Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
• Short rib-polydactyly syndrome, Verma-Naumoff type
• Deafness, congenital onychodystrophy, recessive form
• Syndromic Dystelephalangy
• Deafness symphalangism
• Polytopic Dystelephalangy
• Dystelephalangy
• Deafness -- onychodystrophy -- osteodystrophy -- mental retardation
• Split hand split foot nystagmus
• Hypotrichosis, syndactyly and retinal degeneration
• Deafness onychodystrophy dominant form
• Short stature -- Robin sequence -- cleft mandible -- hand anomalies -- clubfoot
• Anophthalmos with limb anomalies
• Polydactyly visceral anomalies cleft lip palate
• Spastic paraplegia epilepsy mental retardation
• Mental retardation -- contractural arachnodactyly
• Microcephaly with spastic quadriplegia
• Mental retardation -- nasal hypoplasia -- obesity -- genital hypoplasia
• Mental retardation -- short stature -- absent phalanges
• Onychonychia -- hypoplastic distal phalanges
• Split hand/foot malformation X-linked
• Micromelic dysplasia -- dislocation of radius
• Reductional transverse limb defects
• Short limbs -- abnormal face -- congenital heart disease
• ATRUS syndrome
• Aural atresia -- multiple congenital anomalies -- mental retardation
• Congenital heart disease radio ulnar synostos mental retardation
• Lymphoedema tarda
• Hypodontia and Dupuytren contracture
• Unusual facies, macrocephaly, aplasia of corpus callosum, seizures, hypertrichosis, claw hands and overlapping fingers
• Limb reduction defect (generic term)
• Facio-auriculo-radial dysplasia
• Posterior tibial tendon rupture
• Carpal Tunnel Syndrome
• Hereditary Spastic Paraplegia
• Quadriplegia
• Plantar Fasciitis
• Tarsal tunnel
• Spinal muscular atrophy, type 3
• Spinal muscular atrophy with respiratory distress 1
• Spinal muscular atrophy type 2
• Spinal muscular atrophy, type I, with congenital bone fractures
• Spinal muscular atrophy, Ryukyuan type
• Cerebral Palsy, Spastic Quadriplegic, 1
• Cerebral Palsy, Spastic Quadriplegic, 2
• Cerebral Palsy, Spastic Quadriplegic, 3
• Microcephaly -- microphthalmia -- ectrodactyly of lower limbs -- prognathism
• Bowed legs
• Achilles tendon contracture
• Hallux valgus
• Heberden's nodes
• Homans' sign
• Osler's nodes
• Athlete's foot
• Fungal nail infections
• Paronychia
• Arm injury
• Acrocyanosis
• Carpopedal spasm
• Footdrop
• Orofaciodigital syndrome, Shashi type
• Orofaciodigital syndrome type1
• Oral facial digital syndrome, type 4
• Orofaciodigital syndrome, type 3
• Sugarman syndrome
• Orofaciodigital syndrome type 10
• Orofaciodigital syndrome type Thurston type
• Orofaciodigital syndrome type I
• OFD syndrome type Figuera
• Oral facial digital syndrome
• Oral facial digital syndrome, type IV
• OFD syndrome type IX
• OFD syndrome type 8
• Edwards Syndrome
• Thurston syndrome
• Orofaciodigital syndrome Thurston type
• Orofaciodigital syndrome, Gabrielli type
• Oligodactyly -- tetramelic postaxial
• Adactylia unilateral dominant
• Hereditary koilonychia
• Fibular aplasia
• Compulsive finger picking
• Aniridia -- absent patella
• Poland Syndrome
• Nail dysplasia
• Jackson-Weiss Syndrome
• Microcephaly albinism digital anomalies syndrome
• Spinal muscular atrophy -- Dandy-Walker complex -- cataracts
• SPG
• Split hand -- split foot
• Split hand -- split foot -- deafness
• Spinal muscular atrophy, scapuloperoneal
• Hypoglossia -- Hypodactylomelia
• Hypoglossia -- Hypomelia
• Hypoglossia -- Hypodactylia
• Glossopalatine Ankylosis -- Hypoglossia -- Hypodactylomelia
• Glossopalatine Ankylosis -- Hypoglossia -- Hypomelia
• Glossopalatine Ankylosis -- Hypoglossia -- Hypodactylia
• Intraoral Bands -- Hypoglossia -- Hypodactylomelia
• Intraoral Bands -- Hypoglossia
• Aglossia-Hypoactylia syndrome
• Micrognathia with Peromelia
• Aglossia-Adactylia syndrome
• Oromandibular and Limb Hypogenesis Syndrome, Type III
• Oromandibular and Limb Hypogenesis Syndrome, Type II
• Oromandibular and Limb Hypogenesis Syndrome, Type I
• Keratosis palmoplantaris -- corneal dystrophy
• Congenital contractures
• Metatarsus adductus
• Synostoses, tarsal, carpal, and digital
• Wilms tumour and radial bilateral aplasia
• Brachydactyly type B
• Brachydactyly type C
• Brachydactyly type E
• Brachydactyly type A1
• Brachydactyly type A3
• Brachydactyly type A6
• Brachydactyly types B and E combined
• Brachydactyly with hypertension
• Brachydactyly, type A5, nail dysplasia
• Brachydactyly preaxial with hallux varus and thumb abduction
• Brachydactyly, long thumb type
• Brachydactyly -- scoliosis -- carpal fusion
• Brachydactyly type A2
• Brachydactyly, type a7
• Brachydactyly -- absence of distal phalanges
• Brachydactyly -- tibial hypoplasia
• Brachydactyly -- arterial hypertension
• Brachydactyly, type B2
• Brachydactyly type D
• Split hand split foot mandibular hypoplasia
• Sensory neuropathy type 1
• Neuropathy hereditary sensory and autonomic type 1
• Hereditary sensory and autonomic neuropathy 3
• Hereditary sensory neuropathy type 1
• Hereditary sensory neuropathy type 2
• Polyneuropathy -- hand defect
• Brachymetatarsus IV
• Adducted thumbs Dundar type
• Lissencephaly type III -- metacarpal bone dysplasia
• Saethre-Chotzen Syndrome
• Acrocephalopolydactyly II
• Carpenter syndrome
• Acrocephalosyndactyly II
• Acrocephalosyndactyly
• Acrocephalopolydactyly
• Acrocephalopolysyndactyly type III
• Acrocephalosyndactyly type 3 (ACPS 3)
• Acrocephalopolysyndactyly, type 2 (ACPS 2)
• Acrocephalopolydactyly -- Cardiac Disease -- Ear, Skin and Lower Limb Defects
• ACPS III
• Trichorhinophalangeal Syndrome Type II
• Trichorhinophalangeal Syndrome Type I
• Trichorhinophalangeal syndrome type 1
• Trichorhinophalangeal syndrome type 3
• Trichorhinophalangeal Syndrome Type III
• Trichorhinophalangeal syndrome type 2
• Tricho-onychic dysplasia
• Tricho-odonto-onychial dysplasia
• Onychotrichodysplasia and neutropenia
• Multiple congenital contractures
• Heart defects -- limb shortening
• Triphalangeal thumb, non opposable
• Tricho-retino-dento-digital syndrome
• Tricho odonto onycho dermal syndrome
• Callosities, hereditary painful
• Neuropathy, hereditary motor and sensory, LOM type
• Neuropathy, hereditary motor and sensory, Okinawa type
• Dejerine-Sottas Syndrome
• Hypertrophic neuropathy of Dejerine-Sottas
• Dejerine-Sottas disease
• Heart-hand syndrome, Spanish type
• Heart-hand syndrome, Slovenian type
• Holt-Oram Syndrome
• Wieacker-Wolff Syndrome
• Insulin resistance, short fifth metacarpals
• Radial ray agenesis
• Spastic paraplegia nephritis deafness
• Pelvic dysplasia arthrogryposis of lower limbs
• Rolled and spiral hairs -- palmoplantar keratoderma
• Radioulnar synostosis mental retardation hypotonia
• Ichthyosis tapered fingers midline groove up
• Cleft palate cardiac defect ectrodactyly
• Cleft palate colobomata radial synostosis deafness
• Seckel syndrome 4
• Seckel syndrome 1
• Seckel syndrome 2
• Seckel syndrome 3
• Preaxial polydactyly type III
• Seckel syndrome
• Seckel-like syndrome, type Buebel
• Pili torti -- onychodysplasia
• Acroosteolysis dominant type
• Hajdu-Cheney Syndrome
• Gordon Syndrome
• Adams-Oliver Syndrome
• Rubinstein-Taybi Syndrome
• Arthrogryposis, distal, type 2A
• Freeman-Sheldon Syndrome
• Whistling face syndrome
• Arthrogryposis, distal, type 2B
• Epidermolysis bullosa, pretibial
• Epidermolysa bullosa simplex and limb girdle muscular dystrophy
• Epidermolysis Bullosa Dystrophica, Pretibial
• Leukonychia totalis -- trichilemmal cysts -- cilliary dystrophy
• Onychotrichodysplasia, chronic neutropenia and mental retardation syndrome
• Ankle defects short stature
• Camptodactyly-ichthyosis syndrome
• Congenital ichthyosiform erythroderma
• Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
• Congenital ichthyosis, microcephalus, quadriplegia
• Congenital Hemidysplasia with Ichthyosiform erythroderma and Limbs Defects
• Fingerprints absence -- congenital milia
• Arthrogryposis -- hyperkeratosis, lethal form
• Arthrogryposis Distal
• Arthrogrypotic hand abnormality and sensorineural hearing loss
• Arthrogryposis-like disorder
• Arthrogryposis due to muscular dystrophy
• Arthrogryposis -- ophthalmoplegia -- retinopathy
• Arthrogryposis IUGR thoracic dystrophy
• Arthrogryposis -- renal dysfunction -- cholestasis syndrome
• Arthrogryposis-like hand anomaly -- sensorineural deafness
• Radial deficiency tibial hypoplasia
• Campomelic dysplasia
• Campomelic dwarfism
• Camptomelic syndrome
• Camptomelic dysplasia II
• Campomelic Syndrome
• Camurati Engelmann disease, type 2
• Camurat-Engelmann disease, type 2
• Camurati-Engelmann Disease
• Skin Creases, Multiple Benign Ring-Shaped, of Limbs
• Multiple Benign Ring-Shaped Creases on Limbs
• Cleft lip palate incisor and finger anomalies
• Hydrocephaly tall stature joint laxity
• Hydrocephaly tall stature joint laxity and kyphoscoliosis
• Distal myopathy, Welander type
• Microcephaly syndactyly brachymesophalangy
• Progressive neurodegeneration -- joint laxity -- cataract
• Keratosis palmoplantaris -- periodontopathia -- onychogryposis
• Palmoplantar Keratoderma
• Congenital dislocation of the patella
• Hypogonadotropic hypogonadism -- syndactyly
• Duane-radial ray syndrome
• Legg-Calve-Perthes syndrome
• Carpal deformity -- micrognathia -- microstomia
• Camptodactyly -- joint contractures and facial skeletal dysplasia
• Brachydactyly -- elbow, wrist dysplasia
• Double fingernail of fifth finger
• Cleft lip palate -- oligodontia -- syndactyly -- pili torti
• Craniosynostosis Fontaine type
• Achenbach syndrome
• Acheiropodia
• Ulna Hemimelia
• Radial Hemimelia
• Fibular Hemimelia
• Hemimelia
• Lipoedema
• Keratosis Palmoplantaris -- Esophageal Carcinoma
• Keratosis Palmaris Et Plantaris with Esophageal Cancer
• Tylosis -- oesophageal carcinoma
• Oral Leukoplakia Associated with Tylosis and Esophageal Carcinoma
• Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 1
• Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate
• Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 3
• Sjogren-Larsson syndrome
• Distal myopathy with vocal cord weakness
• Woolly hair -- palmoplantar keratoderma -- dilated cardiomyopathy
• Cartilaginous -- arthritic -- ophthalmic -- deafness syndrome
• Bowler's finger syndrome
• Burning feet syndrome
• Hairy elbows syndrome
• Distal myopathy with posterior leg and anterior upper limb involvement
• Hereditary inclusion body myopathy -- joint contractures -- ophthalmoplegia
• Scapuloperoneal amyotrophy
• Scapuloperoneal myopathy, X-linked dominant
• Amyotrophy, neurogenic scapuloperoneal, New England type
• Scapuloperoneal syndrome, neurogenic, Kaeser type
• Scapuloperoneal myopathy, MYH7-related
• Myopathy, early-onset with fatal cardiomyopathy
• Myopathy, X-linked with postural muscle atrophy
• Laing distal myopathy
• Desmin-related myopathy with Mallory body-like inclusions
• Minicore myopathy, antenatal onset, with arthrogryposis
• Myopathy mitochondrial -- cataract
• Myopathy congenital multicore with external ophthalmoplegia
• Myopathy with lactic acidosis and sideroblastic anemia
• Native American myopathy
• Minicore myopathy, moderate, with hand involvement
• Inclusion body myopathy 3, autosomal dominant
• Desmin related myopathy
• Distal myopathy, Markesbery-Griggs type
• Hereditary carnitine deficiency syndrome, myopathic
• Myopathy, X-linked, with excessive autophagy
• Welander distal myopathy, Swedish type
• Nemaline myopathy
• Carnitine palmitoyl transferase II deficiency, myopathic
• Congenital myopathy
• Myopathy, myotubular
• Myopathy, congenital fiber-type disproportion
• Scapuloperoneal myopathy
• Centronuclear myopathy, congenital
• Diffuse idiopathic skeletal hyperostosis
• Nemalin myopathy, late onset type
• Nemaline myopathy, early onset type
• Bethlem myopathy
• Myopathy tubular aggregates
• Miyoshi myopathy
• Distal myopathy
• Inclusion body myopathy, 2 autosomal recessive
• Landouzy-Dejerine muscular dystrophy
• Emery-Dreifuss muscular dystrophy, dominant type
• Muscular dystrophy congenital, merosin negative
• Muscular dystrophy, congenital, merosin-positive
• Muscular dystrophy -- white matter spongiosis
• Scleroatonic muscular dystrophy
• Muscular Dystrophy -- Late Onset
• Hypotonic sclerotic muscular dystrophy
• Congenital muscular dystrophy syringomyelia
• Muscular dystrophy, congenital, type 1C
• Facioscapulohumeral Muscular Dystrophy -- Sensorineural Hearing Loss
• Scapuloperoneal Syndrome
• Muscular Dystrophy, Emery Dreifuss
• Muscular dystrophy congenital, with integrin deficiency
• Fryns Syndrome
• Diaphragmatic hernia -- upper limb defects
• Diaphragmatic defect -- limb deficiency -- skull defect
• Diaphragmatic agenesis -- radial aplasia -- omphalocele
• Humeroradioulnar synostosis
• Meningoencephalocele -- arthrogryposis -- hypoplastic thumb
• Wilms tumor and radial bilateral aplasia
• Hairy palms and soles
• Decreased ankle and knee reflexes
• Decorticate posture
• Decorticate posture in children
• Porokeratosis plantaris, palmaris, et disseminata
• Hypodontia -- nail dysgenesis
• Duplication of leg mirror foot
• Punctate acrokeratoderma -- freckle-like pigmentation
• Tetra-amelia with ectodermal dysplasia and lacrimal duct abnormalities
• Pseudohermaphroditism, female -- skeletal anomalies
• Mirror hand syndrome
• Leg Duplication -- Mirror Foot
• Serpentine fibula -- polycystic kidney syndrome
• Short tarsus -- absence of lower eyelashes
• Limb dystonia
• Congenital heart disease -- radio ulnar synostosis -- mental retardation
• Crossed polydactyly
• Al Gazali Hirschsprung syndrome
• Hirschsprung disease type D brachydactyly
• Hirschsprung disease -- polydactyly -- heart disease
• Cornelia de Lange Syndrome
• Cornelia de Lange syndrome 2
• Cornelia de Lange syndrome 1
• Coffin-Siris Syndrome
• Femoral Hypoplasia-Unusual Facies Syndrome
• Vildervanck syndrome 4
• Miller Syndrome
• Genee-Wiedemann syndrome
• Anetoderma, perifollicular
• Craniosynostosis contractures cleft
• Neuropathy, distal hereditary motor, Jerash type
• Preaxial polydactyly, type 1
• Keratoderma, Palmoplantar, Diffuse
• Capillary Malformation of the Lower Lip, Lymphatic Malformation of Face and Neck, Asymmetry of Face and Limbs, and Partial/Generalized Overgrowth.
• Anonychia -- onychodystrophy
• Cloverleaf skull micromelia thoracic dysplasia
• Hypodontia dysplasia of nails
• Brachydactyly nystagmus cerebellar ataxia
• Growth deficiency brachydactyly unusual facies
• Polysyndactyly orofacial anomalies
• Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly
• Long thumb, brachydactyly syndrome
• Polydactyly postaxial dental and vertebral
• Microphthalmia -- camptodactyly -- mental retardation
• Symphalangism -- brachydactyly -- craniosynostosis
• T-cell immunodeficiency, congenital alopecia and nail dystrophy
• Onychodystrophy and anonychia with type B brachydactyly and ectrodactyly
• Transverse limb deficiency -- hemangioma
• Carpotarsal osteochondromatosis
• Patau syndrome
• Achondroplasia
• Hairy elbows
• Keratosis palmoplantaris -- adenocarcinoma of the colon
• Congenital pseudoarthrosis
• Eosinophilic synovitis
• Edward Syndrome
• Spastic paraplegia glaucoma precocious puberty
• Fibular dimelia -- diplopodia
• Chondrodysplasia punctata with steroid sulfatase deficiency
• Traumatic amputation
• Adducted thumb syndrome recessive form
• Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia
• Bennett fracture
• Kuster syndrome
• Onchyomycosis
• Distal lateral subungual onychomycosis
• Proximal subungual onychomycosis
• White superficial Onychomycosis
• Endonyx onychomycosis
• Sarcoglycanopathy
• Olecranon bursitis
• Dyshidrotic dermatitis
• Bicipital tendinosis
• Bicipital tendonitis
• Bicipital syndrome
• Acute idiopathic polyneuritis
• Alpha-sarcoglycanopathy
• Glomus vagale tumors
• Lipomatous hemangiopericytoma
• Keratosis palmoplantaris -- esophageal cancer
• Keratosis palmoplantaris with esophageal cancer
• Pierre Robin sequence -- congenital heart defect -- talipes
• X-linked mental retardation craniofacial abnormal microcephaly club
• Delta-sarcoglycanopathy
• Van Bogaert-Hozay syndrome
• Lymphedema, hereditary
• Epiphyseal dysplasia, multiple
• Multiple epiphyseal dysplasia
• Epiphyseal dysplasia, multiple, 4
• Pachyonychia congenital syndrome type II
• Spondyloepiphyseal dysplasia -- brachydactyly and distinctive speech
• Adactylia unilateral
• Nephronophtisis familial, adult form -- spastic quadriparesia
• Renal dysplasia -- limb defects syndrome
• Ectodermal dysplasia, 'pure' hair-nail type
• Split-Hand/Foot Malformation with Long Bone Deficiency 3
• Split-Hand/Foot Malformation with Long Bone Deficiency 2
• Dyschromatosis Universalis Hereditaria 1
• Dyschromatosis Universalis Hereditaria 2
• Genochondromatosis II
• Genochondromatosis
• Richieri-Costa Pereira syndrome
• Spondyloepimetaphyseal Dysplasia, Aggrecan Type
• Cousin Walbrau Cegarra Syndrome
• Peromelia
• Jussieu syndrome
• Oromandibular and Limb Hypogenesis Syndrome, Type V
• Oppenheim's dystonia
• Zechi-Ceide Syndrome
• Split-hand deformity
• Split Hand/Split Foot Malformation
• Primrose Syndrome
• Plasmalogenes synthesis deficiency isolated
• Piepkorn karp hickoc syndrome
• Ectodermal dysplasia -- absent dermatoglyphs
• Fischer Syndrome
• Brachydactyly, absent pectoral muscles and agenesis/hypoplasia of kidneys
• Blepharophimosis with ptosis, syndactyly, and short stature
• Talo-patello-scaphoid osteolysis, synovitis, and short fourth metacarpals
• Acanthokeratodermia
• Hydrocephalus skeletal anomalies
• Barrow-Fitzsimmons Syndrome
• Thumb deformity
• Overgrowth radial ray defect arthrogryposis
• Esophageal Atresia, Coloboma, Clubfoot
• Split-Hand/Foot Malformation with Long Bone Deficiency 1
• Talonavicular coalition
• Apelt-Gerkin-Lenz Syndrome
• Kirner Deformity
• Abuelo Forman Rubin Syndrome
• Autosomal Recessive Tetra-Amelia
• Focal Familial Palmoplantar Keratoderma with Punctate Hyperkeratosis of the Palmar Creases
• Tracheoesophageal fistula symphalangism
• Bennion-Patterson Syndrome
• Mirror polydactyly -- vertebral segmentation -- limbs defects
• Mental mixed retardation deafnes clubbed digits
• CRMO, juvenile
• Scapuloperoneal syndrome, neurogenic type
• Macrodactyly of the hand
• Humeroradial synostosis syndrome
• Spinal shock
• Epidermolytic palmoplantar keratoderma Vorner type
• Lundberg I
• Chondrodystrophia punctata, autosomal dominant
• Paraplegia -- brachydactyly -- cone-shaped epiphysis
• Hypoplasia of the tibia with polydactyly
• Keratosis palmoplantaris striata 2
• Short stature, Brussels type
• Pectus excavatum macrocephaly dysplastic nails
• Keratosis palmoplantaris papulosa
• Alopecia congenita keratosis palmoplantaris
• Keratosis palmoplantaris striata 1
• Keratosis palmoplantaris striata 3
• Keratoderma palmoplantaris transgrediens et progrediens
• Keratosis palmoplantaris striata
• Robinow Syndrome
• Robinow syndrome, recessive form
• Robinow syndrome, autosomal recessive
• Robinow-like syndrome
• Amelia, autosomal recessive
• Anonychia onychodystrophy brachydactyly type b
• Anonychia
• Anonychia with flexural pigmentation
• Polydactyly postaxial
• Polydactyly alopecia seborrheic dermatitis
• Polydactyly preaxial type 1
• Polydactyly, preaxial IV
• Polydactyly cleft lip palate psychomotor retardation
• Syndactyly -- preaxial polydactyly -- sternal deformity
• Brain malformation -- congenital heart disease -- postaxial polydactyly
• Hypopituitarism postaxial polydactyly
• Short rib-polydactyly syndrome, Majewski type
• Short rib-polydactyly syndrome, Saldino-Noonan type
• Ulnar hypoplasia lobster claw deformity of feet
• Short rib -- polydactyly syndrome
• Scalp defects -- postaxial polydactyly
• Mirror polydactyly -- segmentation and limbs defects
• Syndactyly -- polydactyly -- ear lobe syndrome
• Crossed polydactyly type 1
• Anonychia -- ectrodactyly
• Thumb absence -- hypoplastic halluces
• Tibia absent -- polydactyly -- arachnoid cyst
• Ectrodactyly -- polydactyly
• Cortical blindness -- mental retardation -- polydactyly
• Crossed polysyndactyly
• Rigid mask-like face -- deafness -- polydactyly
• Pierre Robin syndrome skeletal dysplasia polydactyly
• Trigonomacrocephaly -- tibial defect -- polydactyly
• Hypothyroidism postaxial polydactyly mental retardation
• Cleft palate -- heart disease -- polydactyly -- absent tibia
• Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia
• Megalencephaly -- polymicrogyria -- post-axial polydactyly -- hydrocephalus
• Mullerian derivatives -- lymphangiectasia -- polydactyly
• Urophathy distal obstructive polydactyly
• Phocomelia ectrodactyly deafness sinus arrhythmia
• Polysyndactyly overgrowth syndrome
• Phocomelia ectrodactyly ear malformation deafness sinus arrhythmia
• Cephalopolysyndactyly
• Limb deficiencies distal micrognathia
• Greig Cephalopolysyndactyly Syndrome
• Short ribs -- craniosynostosis -- polysyndactyly
• Triphalangeal thumb -- polysyndactyly syndrome
• Fibula aplasia complex -- brachydactyly
• Polysyndactyly -- cardiac malformation
• Heart defect, tongue hamartoma and polysyndactyly
• Polysyndactyly type Haas
• Polysyndactyly -- trigonocephaly -- agenesis of corpus callosum
• Corpus callosum agenesis -- polysyndactyly
• Phocomelia -- thrombocytopenia -- encephalocele -- urogenital malformation
• Roberts-SC Phocomelia
• Phocomelia syndrome
• Ectrodactyly
• Frontonasal dysplasia -- phocomelic upper limbs
• Phocomelia -- contractures -- absent thumb
• Ectrodactyly, recessive form
• Ectrodactyly cleft palate syndrome
• Tibial aplasia ectrodactyly
• Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate
• Ectrodactyly dominant form
• Femur bifid with monodactylous ectrodactyly
• Oculo-cerebro-acral, (Roberts-like)-ectrodactyly
• Cleft lip -- palate -- ectrodactyly
• Cleft lip -- palate -- abnormal thumbs -- microcephaly
• Craniosynostosis -- fibular aplasia
• Congenital microgastria limb reduction defect
• Splenogonadal fusion, limb defects, micrognathia
• Acro-pectoro-renal field defect
• Microsomia -- hemifacial -- radial defects
• Radial defect -- Robin sequence
• Spastic paraplegia with precocious puberty
• Limb reduction defect
• Limb transversal defect -- cardiac anomaly
• Eye defects -- arachnodactyly -- cardiopathy
• Upper limb defect eye and ear abnormalities
• Arterial occlusive disease, progressive -- hypertension -- heart defects -- bone fragility -- brachysyndactyly
• Coronal synostosis, syndactyly and jejunal atresia
• Blepharoptosis -- cleft palate -- ectrodactyly -- dental anomalies
• Ectodermal dysplasia -- ectrodactyly -- macular dystrophy
• Fibular aplasia -- ectrodactyly
• Ectrodactyly -- cardiopathy -- dysmorphism
• Short stature -- monodactylous -- ectrodactyly -- cleft palate
• Cleft palate -- cardiac defect -- genital anomalies -- ectrodactyly
• Holoprosencephaly -- ectrodactyly -- cleft lip/palate
• Hydrops ectrodactyly syndactyly
• Ectrodactyly ectrodermal dysplasia
• Anophthalmia -- hand and foot defects -- mental retardation
• Short limbs subluxed knees cleft palate
• Cardiac malformation, cleft lip-palate, microcephaly and digital anomalies
• Familial patella aplasia-hypoplasia
• Palant cleft palate syndrome
• Dysraphism -- cleft lip palate -- limb reduction defects
• EEC syndrome without cleft lip/palate
• Leg absence -- deformity -- cataract
• Contractures -- ectodermal dysplasia -- cleft lip palate
• Tibial hemimelia -- cleft lip/palate
• Multiple Hereditary Exostoses
• Exostoses, multiple
• Exostoses
• Exostoses, multiple, type 1
• Exostoses, multiple, type 3
• Exostoses -- anetodermia -- brachydactyly type E
• Dupuytren subungual exostosis
• Uropathy distal obstructive polydactyly
• Ellis-van Creveld syndrome
• Chondroectodermal dysplasia
• Spastic paraplegia -- neuropathy -- poikiloderma
• Fanconi pancytopenia
• Duplication of the thumb, unilateral biphalangeal
• Palmoplantar keratoderma punctate, hereditary
• Palmoplantar keratoderma -- amyotrophy
• Diffuse palmoplantar keratoderma -- acrocyanosis
• Palmoplantar keratoderma -- XX sex reversal -- predisposition to squamous cell carcinoma
• Keratosis palmaris et plantaris -- clinodactyly
• Diffuse palmoplantar keratoderma, Norrbotten dominant type
• Keratoderma palmoplantar, Norrbotten recessive type
• Palmoplantar porokeratosis of Mantoux
• Keratosis palmoplantar periodontopathy
• Keratosis focal -- palmoplantar, gingival
• Leukoencephalopathy -- palmoplantar keratoderma
• Diffuse palmoplantar keratoderma, Bothnian type
• Thost-Unna palmoplantar keratoderma
• Keratoderma palmoplantar -- deafness
• Stuccokeratosis
• Porokeratosis punctata palmaris et plantaris
• Hypokeratosis, palmo-plantar, circumscribed
• Contractures hyperkeratosis lethal
• Hyperkeratosis lenticularis perstans
• Acromelanosis
• Acrorenal syndrome
• Spondylocarpotarsal synostosis
• Hemifacial microsomia macrodactyly
• Camptodactyly -- fibrous tissue hyperplasia -- skeletal dysplasia
• Diaphanospondylodysostosis
• Arachnodactyly -- Intellectual Deficit -- Dysmorphism
• Al Awadi-Raas-Rothschild syndrome
• Spondylohypoplasia arthrogryposis popliteal pterygium
• Achondrogenesis type 1A
• Achondrogenesis type 2
• Achondrogenesis, Langer-Saldino Type
• Achondrogenesis type 1B
• X-linked hydrocephalus spectrum
• Achondrogenesis type 1A and 1B
• Atelosteogenesis, type 1
• Atelosteogenesis Type III
• Atelosteogenesis, type 2
• Achondrogenesis
• Pyknoachondrogenesis
• Achondrogenesis, type 3
• Achondrogenesis, type 4
• Pigmented purpuric eruption
• Aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits and nails
• Camptodactyly syndrome, Guadalajara type 1
• Goodman camptodactyly
• Spondylo camptodactyly syndrome
• Tel-Hashomer camptodactyly syndrome
• Syncamptodactyly -- scoliosis
• Camptodactyly syndrome, Guadalajara type 2
• Camptodactyly syndrome, Guadalajara type III
• Camptodactyly syndrome, Guadalajara type 3
• Camptodactyly, tall stature, and hearing loss syndrome
• Camptodactyly -- taurinuria
• Camptodactyly -- vertebral fusion
• Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia
• Contractures, congenital, torticollis and malignant hyperthermia
• Metacarpals 4 and 5 fusion
• Radius absent -- anogenital anomalies
• Hanhart syndrome type II
• Hanhart syndrome type IV
• Hanhart Syndrome
• Hanhart syndrome type III
• Hanhart syndrome type I
• Osteoarthropathy of fingers, familial
• Acropustulosis
• L1 Syndrome
• Macrocephaly pigmentation large hands feet
• Larsen syndrome, dominant type
• Larsen-like osseous dysplasia -- dwarfism
• Larsen-like syndrome, lethal form
• Eyebrows duplication syndactyly
• Larsen syndrome
• Larsen syndrome, recessive type
• Larsen-like syndrome, lethal type
• Immunodeficiency with short limb dwarfism
• Pterygium colli -- mental retardation -- digital anomalies
• Brachmann-De Lange Syndrome
• Ainhum
• Acromesomelic dysplasia
• Langer mesomelic dysplasia
• VATER association
• Whelan syndrome
• Varadi Papp syndrome
• Mohr syndrome
• Leri-Weil syndrome
• Craniofrontonasal dysplasia
• Conradi-Hunermann syndrome
• Patella aplasia, coxa vara, tarsal synostosis
• Macrodactyly of the foot
• Lymphedema distichiasis syndrome
• Lymphedema -- ptosis
• Lymphedema, congenital
• Pachyonychia congenital syndrome
• Popliteal pterygium syndrome
• Green nail syndrome
• Hallux Rigidus
• Spondylometaphyseal dysplasia -- cone-rod dystrophy
• Spondylometaphyseal dysplasia, axial
• Spondylometaphyseal dysplasia, Algerian type
• Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
• Spondylometaphyseal dysplasia, east-African type
• Spondylometaphyseal dysplasia, Sedaghatian type
• Spondylometaphyseal dysplasia, 'corner fracture' type
• Spondylometaphyseal dysplasia with combined immunodeficiency
• Spondylometaphyseal dysplasia, X-linked
• VACTERL with hydrocephalus, X-linked
• VACTERL association
• VACTERYL hydrocephaly
• VACTERL association with hydrocephaly, X-linked
• Stickler's syndrome
• Stickler Syndrome
• Stickler Syndrome, type II
• Stickler Syndrome, type III
• Stickler Syndrome, type I
• Multiple synostosis syndrome
• Isaacs syndrome
• Tooth and Nail syndrome
• Yellow nail syndrome
• Kenny-Caffey Syndrome
• Kenny-Caffey syndrome, Type 2
• Kenny-Caffey syndrome, Type 1
• Short stature -- contractures -- hypotonia
• Craniomicromelic syndrome
• Digitorenocerebral syndrome
• Leukonychia totalis
• Knuckle pads, leukonychia and sensorineural deafness
• Meckel syndrome type 2
• Nephrosis -- deafness -- urinary tract -- digital malformation
• Microcephaly -- oculo-digito-esophageal-duodenal syndrome (MODED)
• Meckel Syndrome
• Meckel syndrome type 3
• Meckel syndrome, type 5
• Popliteal pterygium syndrome, lethal type
• Pterygium, Popliteal, lethal type
• Spondylohypoplasia, arthrogryposis and popliteal pterygium
• Erythermalgia
• Anonychia -- microcephaly
• Skeletal dysplasia, San Diego type
• Pelvic-shoulder dysplasia
• Femur-fibula-ulna syndrome
• Spondyloepimetaphyseal dysplasia with joint laxity
• Tarsal carpal coalition syndrome
• Teeth noneruption of with maxillary hypoplasia and genu valgum
• Odontomicronychial dysplasia
• Septooptic dysplasia -- digital anomalies
• Odontoonychodermal dysplasia
• Primerose syndrome
• Radio-ulnar synostosis type 2
• Ankyloglossia -- heterochromia -- clasped thumbs
• Oculodigitoesophagoduodenal syndrome
• Spastic paraplegia with Kallmann syndrome
• Syndactyly -- cataract -- mental retardation
• Facial dysmorphism -- shawl scrotum -- joint laxity syndrome
• Thumb deformity, alopecia, pigmentation anomaly
• Tsao-Ellingson syndrome
• Odonto onycho dysplasia with alopecia
• Dinno-Shearer-Weisskopf syndrome
• Otoonychoperoneal syndrome
• Spondyloepimetaphyseal dysplasia, micromelic
• Marfanoid -- mental retardation syndrome autosomal
• Ectodermal dysplasia -- neurosensory deafness
• Spondyloepimetaphyseal dysplasia congenita, Iraqi
• Thumb absent -- short stature -- immune deficiency
• Pachyonychia congenita recessive
• Humerus, trochlea, aplasia of
• Sacral plexopathy
• Skeletal dysplasia -- coarse facies -- mental retardation
• Parkes-Weber syndrome I
• Chondrodysplasia punctata, Sheffield type
• Chondrodysplasia punctata, tibia-metacarpal type
• Chondrodysplasia punctata, brachytelephalangic
• Chondrodysplasia Punctata, Rhizomelic type
• Chondrodysplasia punctata, humero-metacarpal type
• Rhizomelic chondrodysplasia punctata, type 1
• Rhizomelic chondrodysplasia punctata, type 2
• Rhizomelic chondrodysplasia punctata, type 3
• Iris coloboma, macrocephaly, agenesis of the corpus callosum, brachydactyly and mental retardation
• Coloboma of macula, type B brachydactyly
• Lethal congenital contracture syndrome 1
• Lethal congenital contracture syndrome 2
• Accessory deep peroneal nerve
• Common peroneal nerve dysfunction
• Hand-foot-uterus syndrome
• Metaphyseal chondrodysplasia Spahr type
• Metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands
• Leukoencephalopathy -- metaphyseal chondrodysplasia
• Metaphyseal chondrodysplasia, recessive type
• Unusual facies, digital anomalies, and supernumerary teeth
• Familial hematuria, autosomal dominant -- retinal arteriolar tortuosity -- contractures
• Neuronopathy, distal hereditary motor, type IIB
• Gnathodiaphyseal dysplasia
• Long thumb brachydactyly, maxillary hypoplasia, mental retardation and unusual facies
• Unusual facies, preauricular pits, fifth finger clinodactyly and tetralogy of Fallot
• Digital arthropathy-brachydactyly, familial
• Acroparesthesia syndrome
• Osteoporosis -- macrocephaly -- blindness -- joint hyperlaxity
• Acropectoral syndrome
• Acrodysplasia scoliosis
• Acropectorovertebral dysplasia
• Acromesomelic dysplasia, Maroteaux type
• Acrofacial dysostosis Preis type
• Amelo-onycho-hypohidrotic syndrome
• Clayton-Smith Donnai syndrome
• Bowing of legs, anterior, with dwarfism
• Brachydactylous dwarfism, Mseleni type
• Short stature locking fingers
• Spondylo-humero-femoral dysplasia
• Double Upper and Lower Lip -- Hypertelorism -- Ptosis -- Blepharophimosis -- clinodactyly
• Syndactyly type 1 -- microcephaly -- mental retardation
• Macrocephaly -- short stature -- paraplegia
• Onycho-tricho-dysplasia -- neutropenia
• Microcephaly brachydactyly kyphoscoliosis
• Tetramelic deficiencies -- Ectodermal dysplasia -- deformed ears -- other abnormalities
• Ulna hypoplasia with mental retardation
• Blepharophimosis ptosis esotropia syndactyly short
• Fibular hypoplasia or aplasia -- femoral bowing -- oligodactyly
• Fuhrmann-Rieger-de Sousa syndrome
• Bone dysplasia Moore type
• Bowing of Long Bones, Asymmetrical and Symmetrical
• Theodor-Hertz-Goodman syndrome
• Limb-mammary syndrome
• Robin sequence oligodactyly
• Hallux limitus
• Macrocephaly, rhizomelia and conductive hearing loss
• Hydrops fetalis -- anaemia -- immune disorder -- absent thumb
• Craniometadiaphyseal dysplasia, wormian bone type
• Dauwerse-Peters syndrome
• Growth retardation mental retardation phalangeal hypoplasia
• Blepharophimosis, ptosis, polythelia and brachydactyly
• Osteoporosis, severe -- shortened long bones -- white sclerae
• Krieble Bixler syndrome
• Mesomelic dysplasia, Camera type
• Mesomelia radial hypoplasia bifid thumb unusual facies
• Infantile spasms -- broad thumbs
• Idiopathic edema
• Hereditary vascular retinopathie -- Raynaud phenomenon -- migraine
• Ossification anomalies -- psychomotor development
• Houlston ironton temple syndrome de
• Koussef nichols syndrome
• Toe syndactyly, telecanthus, and anogenital and renal malformations
• Hand-Foot-Mouth Syndrome
• Lethal congenital contracture syndrome (LCCS)
• Unusual facies, hypotonia, mental retardation and radioulnar synostosis
• Double nails on the fifth toe
• Bruck syndrome 1
• Bruck syndrome, 2
• Craniofacial -- deafness -- hand syndrome
• Radio digito -- facial dysplasia
• Short limb dwarf mental retardation myopia
• Monomelic Amyotrophy
• Podagra
• Buerger's disease
• Chilblain
• McCune-Albright Syndrome
• Marfan syndrome
• Onychogryphosis
• Osteochondritis Dissecans
• Familial Articular Chondrocalcinosis
• Clubfoot
• Apert syndrome
• Whitlow
• Meralgia paresthetica
• Morton's Neuroma
• Brachial Neuritis
• Compartment Syndrome
• Nail-Patella Syndrome
• Acrodysostosis
• Cronkhite-Canada Syndrome
• Dyschondrosteosis
• MASA Syndrome
• Sclerosteosis
• Weismann-Netter-Stuhl Syndrome
• Townes-Brocks Syndrome
• Brailsford
• Brachymesophalangy 2 and 5
• Brachymesomelia-renal syndrome
• Cerebrorenodigital syndrome
• Elephant man in context of NF
• Ruvalcaba-Myhre-Smith Syndrome
• Zimmerman-Laband syndrome
• Antley-Bixler Syndrome
• Pachydermoperiostosis
• Baller-Gerold Syndrome
• Nager Syndrome
• Pallister-Hall Syndrome
• Meleda Disease
• Laband Syndrome
• Laurence-Moon Syndrome
• Schinzel Syndrome
• Roberts Pseudothalidomide Syndrome
• C-like syndrome
• Chondrodystrophia calcificans congenita
• Conradi-Huenermann Syndrome
• Acrosphenosyndactylia
• Jequier-Kozlowski-skeletal dysplasia
• Pachyonychia congenital syndrome type I
• Chondrodystrophy
• Chondrodysplasia, Grebe type
• Metaphyseal chondrodysplasia Schmid type
• Fingerprints absence -- syndactyly -- milia
• Eyebrow Duplication -- Stretchable Skin -- Syndactyly
• Stuve-Wiedemann syndrome
• Stuve-Wiedemann dysplasia
• Camera Costa Syndrome
• Stoll Levy Francort Syndrome
• Freire-Maia syndrome
• Pfeiffer-Weber-Christian syndrome
• Edwards-Gale Syndrome
• Claudication pain
• Dancing Eye syndrome
• Hip dysplasia -- enchondromata -- ecchondromata
• Segawa syndrome, autosomal dominant
• Segawa syndrome, autosomal recessive
• Limited cutaneous systemic sclerosis
• Meige's lymphedema
• Craniofacial conodysplasia
• Eiken syndrome
• Erdheim-Chester syndrome
• Gamborg nielsen syndrome
• Gollop Coates syndrome
• Goossens-Devriendt syndrome
• Kumar levick syndrome
• Levy-Yeboa Syndrome
• Madelung deformity
• MADSAM
• Mandibuloacral dysplasia
• Mesomelic dysplasia, Savarirayan type
• Metaphyseal dysplasia, Braun-Tinschert type
• Morava-Mehes syndrome
• Ribbing disease
• Rudiger syndrome
• Segawa Syndrome
• Trigger thumb
• Ribbing syndrome
• Rot-Bernhardt syndrome
• Satoyoshi syndrome 2
• Schafer syndrome
• Shell nail syndrome
• Tizzard syndrome
• Troell-Junet syndrome
• Wiedemann-Tolksdorf syndrome
• Skewfoot
• Acrocapitofemoral dysplasia
• Acro coxo mesomelic dysplasia
• Acrofacial dysostosis autosomal recessive
• Acrofacial dysostosis postaxial, atypical
• Spondyloepimetaphyseal dysplasia, genevieve type
• Brunzell syndrome
• Bruck syndrome
• Odonto-tricho-ungual-digito-palmarn syndrome
• Whistling face syndrome, recessive form
• Grob syndrome
• Howship-Romberg syndrome
• Hunter-Fraser syndrome
• Ives-Houston syndrome
• Kashin-Bek disease
• Macrodactyly -- Hemihypertrophy -- Connective tissue nevi syndrome
• Majocchi disease
• McLetchie-Aikens syndrome
• Moynahan syndrome III
• Phillips-Griffiths syndrome
• Pratesi syndrome
• Renon-Delille syndrome
• Cardiomelic syndrome Stratton Koehler type
• Richieri-Costa-Orquizas syndrome
• Ectodermal dysplasia, Margarita type
• De Quervains' disease
• Billet-Bear syndrome
• Charlie M syndrome
• Pseudoainhum
• Infantile digital fibromatosis
• Familial streblodactyly
• Barnicoat-Baraitser syndrome
• Cleidorhizomelic syndrome
• Cortes-Lacassie syndrome
• Horn-Kolb syndrome
• Ho Kaufman-Mcalister syndrome
• Lipodermatosclerosis
• Acrofacial dysostosis -- ambiguous genitalia
• Acrorenal syndrome recessive
• Langer-Nishino-Yamaguchi syndrome
• Blethen-Wenick-Hawkins syndrome
• Christian-Demyer-Franken syndrome
• Hypoplastic thumb -- mullerian aplasia
• Filaminopathy, autosomal dominant
• Dysostosis peripheral
• Kantaputra-Gorlin syndrome
• Bruyn-Scheltens syndrome
• Johnson-Hall-Krous syndrome
• Jones-Hersh-Yusk syndrome
• Akaba-Hayasaka syndrome
• Cortada-Kousseff-Matsumoto syndrome
• Frints -- De Smet -- Fabry -- Fryns syndrome
• Cataract, alopecia, sclerodactyly
• Calabro syndrome
• Choledochal cyst, hand malformation
• Hypertrichosis brachydactyly obesity and mental retardation
• Idaho syndrome
• Macleod-Fraser syndrome
• Campomelia Cumming type
• Bowing of long bones congenital
• Acral dysostosis -- dyserythropoiesis
• Alopecia universalis -- onychodystrophy -- vitiligo
• Baby rattle pelvic dysplasia
• Landy-Donnai syndrome
• Acanthosis nigricans muscle cramps acral enlargement
• Brachioskeletogenital syndrome
• Hypomelia -- mullerian duct anomalies
• Acromesomelic dysplasia Campailla Martinelli type
• Fraser-Jequier-Chen syndrome
• Cramp-fasciculations syndrome
• Cerebrorenodigital syndrome with limb malformations and triradiate acetabula
• Laurence-Prosser-Rocker syndrome
• Elattoproteus syndrome
• Johnson-Munson syndrome
• Brugsch's syndrome
• Alajouanine syndrome
• Baerensprung disease
• Bartenwerfer syndrome
• Berger paresthesia
• Berndorfer syndrome
• Bluefarb-Stewart syndrome
• Braun-Bayer syndrome
• Bruns-Garland syndrome
• Cervenka's syndrome
• Chapple syndrome
• Milner-Khallouf-Gibson syndrome
• Maroteaux-Fonfria syndrome
• Richieri-Costa-Silveira-Pereira syndrome
• Orstavik-Lindemann-Solberg syndrome
• Pterygium syndrome, X-linked
• Scaphotrapeziotrapezoid arthrodesis
• Humerospinal dysostosis -- congenital heart disease
• Scholte syndrome
• Say syndrome
• Mesomelic dysplasia -- skin dimples
• Samson-Gardner syndrome
• Muller-Barth-Menger syndrome
• Short limb dwarfism, Al Gazali type
• Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch
• Schwartz-Lelek syndrome
• Pfeiffer-Tietze-Welte syndrome
• Howard-Young syndrome
• Rasmussen-Johnsen-Thomsen syndrome
• Harrod Doman Keele syndrome
• Trochlear dysplasia
• Pseudopapilledema -- blepharophimosis -- hand anomalies
• Radio renal syndrome
• Eyebrows duplication of, with stretchable skin and syndactyly
• Hapnes-Boman-Skeie syndrome
• Lateral body wall complex
• Ghosal syndrome
• Aphalangia -- syndactyly -- microcephaly
• Oro acral syndrome
• Chemke-Oliver-Mallek syndrome
• Robin sequence and oligodactyly
• Kaplan-Plauchu-Fitch syndrome
• Richieri-Costa Da Silva syndrome
• Say-Field-Coldwell syndrome
• Auralcephalosyndactyly
• Furlong-Kurczynski-Hennessy syndrome
• Rhizomelic dysplasia Patterson Lowry type
• Dysharmonic skeletal maturation -- muscular fiber disproportion
• Chitty-Hall-Webb syndrome
• Potocki-Shaffer syndrome
• Spondyloepimetaphyseal dysplasia, Missouri type
• Fuhrmann syndrome
• Fontaine-Farriaux-Blanckaert syndrome
• Rhizomelic syndrome
• Impossible syndrome
• Dermatopathia pigmentosa reticularis
• Polyostotic osteolytic dysplasia, hereditary expansile
• Tetraamelia -- multiple malformations
• Goldblatt-Viljoen syndrome
• Elliott-Ludman-Teebi syndrome
• Mononen-Karnes-Senac syndrome
• Diphallus -- rachischisis -- imperforate anus
• Oculo skeletal renal syndrome
• Say-Carpenter syndrome
• Judge-Misch-Wright syndrome
• Metaphyseal acroscyphodysplasia
• Hyperphalangism -- dysmorphy -- bronchomalacia
• Axial mesodermal dysplasia spectrum
• Short limb dwarf lethal, Mcalister Crane type
• Eng Strom syndrome
• Talipes equinovarus
• Thoracolimb dysplasia, Rivera type
• Czeizel-Losonci syndrome
• Manouvrier syndrome
• Shoulder and thorax deformity, congenital heart disease
• Symphalangism with multiple anomalies of hands and feet
• Trueb-Burg-Bottani syndrome
• Thanatophoric dysplasia, Glasgow variant
• Facioskeletalgenital syndrome, Rippberger type
• Santos-Mateus-Leal syndrome
• Sclerocornea, Syndactyly, ambiguous genitalia
• Imaizumi Kuroki syndrome
• Tetraamelia with pulmonary hypoplasia
• Stratton-Parker syndrome
• Temtamy preaxial brachydactyly syndrome
• Faciocardiomelic dysplasia, lethal
• Saito-Kuba-Tsuruta syndrome
• Pseudoachondroplastic dysplasia 2
• Mesomelia
• Omodysplasia type 1
• Spondyloepimetaphyseal dysplasia, Irapa type
• Tollner-Horst-Manzke syndrome
• Ray-Peterson-Scott syndrome
• Buntinx-Lormans-Martin syndrome
• Spondyloperipheral dysplasia -- short ulna
• Metaphyseal dysplasia -- maxillary hypoplasia -- brachydactyly
• Selig-Benacerraf-Greene syndrome
• Singh-Chhaparwal-Dhanda syndrome
• Maroteaux-Verloes-Stanescu syndrome
• Herrmann-Opitz craniosynostosi
• Patterson-Stevenson syndrome
• FACES syndrome
• ECP syndrome
• Daneman Davy Mancer syndrome
• Ischiopatellar dysplasia
• Raine syndrome
• SCARF syndrome
• Fried-Goldberg-Mundel syndrome
• Powell-Chandra-Saal syndrome
• Symphalangism distal
• Oculo cerebro acral syndrome
• Frias syndrome
• Pfeiffer-Mayer syndrome
• Schlegelberger-Grote syndrome
• Sacrococcygeal dysgenesis association
• Familial opposable triphalangeal thumbs duplication
• Aplasia cutis congenita of limbs recessive
• Oslam syndrome
• Oto-Palatal-digital syndrome
• TAU syndrome
• Irons-Bhan syndrome
• McDonough syndrome
• Trigonocephaly -- broad thumbs
• Opthalmo acromelic syndrome
• Astley-Kendall syndrome
• Kasznica-Carlson-Coppedge syndrome
• Tukel syndrome
• Reardon-Hall-Slaney syndrome
• Sackey-Sakati-Aur syndrome
• Freire-Maia odontotrichomelic syndrome
• Culler-Jones syndrome
• Dincsoy-Salih-Patel syndrome
• Collins-Pope syndrome
• Sommer-Hines syndrome
• Tsukuhara syndrome
• Engelhard-Yatziv syndrome
• Sequeiros-Sack syndrome
• Timothy syndrome
• Garret-Tripp syndrome
• Spastic ataxia, Charlevoix-Saguenay type
• Jorgenson-Lenz syndrome
• Fryns-Hofkens-Fabry syndrome
• Kosztolanyi syndrome
• Stoll-Levy-Fancfort syndrome
• Schmitt-Gillenwater-Kelly syndrome
• Ectodermal dysplasia trichoodontoonychial type
• Spranger-Schinzel-Myers syndrome
• Char syndrome
• Houlston-Ironton-Temple syndrome
• Omodysplasia
• Sandhaus Ben-Ami syndrome
• Hoon-Hall syndrome
• Sallis-Beighton syndrome
• Hunter-McAlpine syndrome
• Dejerine-Klumpke syndrome
• Illum syndrome
• Acrokeratoelastoidosis of Costa
• Lanzietri syndrome
• Sclerotylosis
• Rosenberg-Lohr syndrome
• Holzgreve-Wagner-Rehder syndrome
• Lowry syndrome
• Rolland-Desbuquois syndrome
• Multiple synostoses syndrome 1
• Piussan-Lenaert-Mathieu syndrome
• Pseudoaminopterin syndrome
• Erdheim disease II
• Pallister-Ulnar mammary syndrome
• Lowry-Wood syndrome
• Idiopathic intestinal pseudoobstruction
• Acrofacial dysostosis Rodriguez type
• Acromesomelic dysplasia Brahimi Bacha type
• Allain Babin Demarquez syndrome
• Albright like syndrome
• Ampola syndrome
• Al Awadi syndrome
• Acromesomelic dysplasia Hunter Thompson type
• Acrofacial dysostosis Catania form
• ADULT syndrome
• Acrofacial dysostosis, Palagonia type
• Thanatophoric dysplasia
• Buttiens-Fryns syndrome
• Brachytelephalangy, characteristic facies, Kallmann
• Bhaskar-Jagannathan syndrome
• Bagatelle-Cassidy syndrome
• Carnevale-Hernandez-Castillo syndrome
• Crisponi syndrome
• Bazopoulou-Kyrkanidou syndrome
• Blount disease
• BOD syndrome
• Grand-Kaine-Fulling syndrome
• Carnevale-Canun-Mendoza syndrome
• Bellini-Chiumello-Rinoldi syndrome
• Chitty Hall Baraitser syndrome
• Chitayat Meunier Hodgkinson syndrome
• Game-Friedman-Paradice syndrome
• Lower limb anomaly -- ureteral obstruction
• Thin ribs -- tubular bones -- dysmorphism
• Fitzsimmons-Guilbert syndrome
• Roy-Maroteaux-Kremp syndrome
• Maroteaux-Stanescu-Cousin syndrome
• Cranioacrofacial syndrome
• Kurczynski-Casperson syndrome
• Le Marec-Bracq-Picaud syndrome
• Opitz-Reynolds-Fitzgerald syndrome
• Nasodigitoacoustic syndrome
• Cote-Katsantoni syndrome
• Seemanova-Lesny syndrome
• Desbuquois syndrome
• Thieffry and Sorrell Dejerine syndrome
• Lujan-Fryns syndrome
• Reese-Ellsworth syndrome
• Syndactyly, Cenani Lenz type
• Forney Robinson Pascoe syndrome
• Ledderhose disease
• Acrofacial dysostosis, Weyers type
• Ballard syndrome
• Sheffield syndrome
• Camptomelic dysplasia I
• Cortical hyperostosis-syndactyly
• Banki syndrome
• De Lange 1
• Acrorenal mandibular syndrome
• Lambert syndrome
• Kniest-like dysplasia lethal
• GOMBO syndrome
• Marsden syndrome
• Davis syndrome
• Karsch-Neugenbauer syndrome
• SAPHO syndrome
• Grant syndrome
• Tylosis
• Fairbank disease
• Touraine-Solente-Gole syndrome
• Kienbock disease
• Freiberg disease
• Kohler disease
• Sulfatidosis juvenile, Austin type
• Cranioectodermal dysplasia
• Dysplasia epiphysealis hemimelica
• Kohler syndrome
• Bartsocas Papa syndrome
• W syndrome
• Mietens syndrome
• Juberg-Hayward syndrome
• Levine-Critchley syndrome
• Scott syndrome
• Roberts syndrome
• Muckle-Wells syndrome
• Vohwinkel syndrome
• Strudwick syndrome
• Rubinstein-Taybi like syndrome
• Parsonage Turner syndrome
• Ventruto Digirolamo Festa syndrome
• Winter Shortland Temple syndrome
• Weleber Hecht Bigley syndrome
• Yim Ebbin syndrome
• Verloes-David Syndrome
• Wiedemann Oldigs Oppermann syndrome
• Willems De vries syndrome
• Viljone Kallis Voges syndrome
• Verloove Vanhorick Brubakk syndrome
• Verloes Bourguignon syndrome
• Walbaum Titran Durieux Crepin syndrome
• Worster Drought syndrome
• Wallerian degeneration
• Westphal disease
• Von voss Cherstvoy syndrome
• Vertical talus, congenital
• Verloes Van Maldergem Marneffe syndrome
• WT limb blood syndrome
• Worth syndrome
• Zlotogora syndrome
• Wegmann Jones Smith syndrome
• Zerres Rietschel Majewski syndrome
• Schneckenbecken dysplasia
• Elejalde syndrome
• Marie-Bamberg syndrome
• Dahlberg syndrome
• Boomerang dysplasia
• Beemer-Langer syndrome
• Crane-Heise syndrome
• Sillence syndrome
• Rapadilino syndrome
• Parastremmatic dwarfism
• Metachondromatosis
• Ivic Syndrome
• Kuskokwim disease
• Lymphangiectasies and lymphedema Hennekam type
• Lewis (F.) syndrome
• King-Denborough syndrome
• Keutel syndrome
• Pillay syndrome
• Osteoglophonic dwarfism
• Nievergelt syndrome
• Mesomelic dwarfism Reinhardt-Pfeiffer type
• Opsismodysplasia
• Frontometaphyseal dysplasia
• Krause-Kivlin syndrome
• Oromandibular-limb hypogenesis spectrum
• Yunis Varon syndrome
• Lenz Majewski hyperostotic dwarfism
• Focal dermal hypoplasia
• Sirenomelia
• Femoral facial syndrome
• Craniometaphyseal dysplasia, autosomal recessive type
• EEC syndrome
• Fibrochondrogenesis
• Grebe Syndrome
• Beals syndrome
• Hecht syndrome
• Geleophysic dwarfism
• Limb-body wall complex
• Blepharophimosis, ptosis, epicanthus inversus
• Nevus sebaceous of Jadassohn
• TAR syndrome
• Ablepharon macrostomia syndrome
• Spherophakia brachymorphia syndrome
• Van der Woude syndrome
• CHILD syndrome ichthyosis
• Acrofacial dysostosis, Nager type
• Hydrolethalus syndrome
• Silver-Russell dwarfism
• Acrofacial dysostosis atypical postaxial
• Craniosynostosis radial aplasia syndrome
• Van der Woude syndrome 2
• Urogenital adysplasia
• Van Goethem syndrome
• Vasquez Hurst Sotos syndrome
• Urogenital adysplasia, hereditary
• Venencie Powell Winkelmann syndrome
• Upton Young syndrome
• Vagneur Triolle Ripert syndrome
• Van Regemorter Pierquin Vamos syndrome
• Van De Berghe Dequeker syndrome
• Behr syndrome
• Wieacker syndrome
• MSBD syndrome
• Sakati syndrome
• Cayler syndrome
• Oculo-dento-digital dysplasia dominant
• Melorheostosis
• Acro-reno-ocular syndrome
• more types...»

What causes Limb conditions?

Causes of Limb conditions: see causes of Limb conditions

What are the symptoms of Limb conditions?

Symptoms of Limb conditions: see symptoms of Limb conditions

Limb conditions: Testing

Misdiagnosis: see misdiagnosis and Limb conditions.

How is it treated?

Treatments for Limb conditions: see treatments for Limb conditions

Name and Aliases of Limb conditions

Main name of condition: Limb conditions

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